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rs587781362

From SNPedia

Orientationplus
Geno Mag Summary
(GTC;GTC) 0 common in clinvar
Make rs587781362(-;-)
Make rs587781362(-;GTC)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47806279
GeneMSH6
is asnp
is mentioned by
dbSNPrs587781362
ebirs587781362
HLIrs587781362
Exacrs587781362
Varsomers587781362
Maprs587781362
PheGenIrs587781362
hapmaprs587781362
1000 genomesrs587781362
hgdprs587781362
ensemblrs587781362
gopubmedrs587781362
geneviewrs587781362
scholarrs587781362
googlers587781362
pharmgkbrs587781362
gwascentralrs587781362
openSNPrs587781362
23andMers587781362
23andMe allrs587781362
SNP Nexus

SNPshotrs587781362
SNPdbers587781362
MSV3drs587781362
GWAS Ctlgrs587781362
Max Magnitude0
ClinVar
Risk rs587781362(;)
Alt rs587781362(;)
Reference rs587781362(GTC;GTC)
Significance Probable-Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48033420_48033422delCGT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074918.2, RCV000129144.3,